c_Jun (dn)
- Known as:
- c_Jun (dn)
- Catalog number:
- 000045A
- Product Quantity:
- 250ul
- Category:
- -
- Supplier:
- ABM
- Gene target:
- c_Jun ()
Ask about this productRelated products to: c_Jun (dn)
Related articles to: c_Jun (dn)
- 2-Hydroxy ethylmethacrylate (HEMA) is a hydrophilic monomer that may be released from composite resin after polymerization. Little is known about the adverse effects of HEMA on cementoblasts. Therefore, this study investigated the possible mechanisms underlying the cytotoxicity engendered by HEMA on murine cementoblast cell line (OCCM.30). - Source: PubMed
Publication date: 2026/04/01
Lai Wei-JuShen Wen-YingSu Chun ChuanChang Yu-Chao - Vitamin D is traditionally known for bone metabolism and also exerts immunomodulatory effects. Dental pulp stem cells (DPSCs) are essential for pulp repair but are impaired under lipopolysaccharide (LPS)-induced inflammation. Therefore, we examined the dual effects of 1α,25-dihydroxyvitamin D (1α,25(OH)D) on inflammation and osteogenic differentiation in DPSCs. - Source: PubMed
Publication date: 2026/07/01
Song Seong EunYun GiyoungKim Cheul-HongYoon Ji-YoungKim Hee YoungKim Hyae JinKim Eun-Jung - Endothelin-1 (ET-1) has been implicated in inflammatory tissue responses, but its role in osteoblast-mediated inflammation during periodontal inflammation remains unclear. This study investigated whether ET-1 induces cyclooxygenase-2 (COX-2) expression and prostaglandin E (PGE) release in osteoblasts and explored the underlying signaling mechanisms. - Source: PubMed
Publication date: 2026/07/01
Fan Fang-YuVo Thi Thuy TienKuo HsuanTseng Chien-FuLin Wei-NingWu Chia-YuWu Yang-CheYang Chuen-MaoHsiao Li-DerLee I-Ta - Genetic susceptibility to obstructive sleep apnea (OSA) may vary by ancestry. We have conducted a systematic review and random-effects meta-analysis of observational studies (International Prospective Register of Systematic Reviews [PROSPERO] CRD42024548801) to test whether ancestry modifies the associations involving specific genetic polymorphisms and OSA risk and severity. We searched databases until June 2024 for studies examining variants (interleukin-6 (IL6) rs1800795, tumor necrosis factor (TNF) rs1800629, solute carrier family 6 member 4 (serotonin-transporter gene) (SLC6A4) serotonin-transporter-linked polymorphic region (5-HTTLPR)/serotonin transporter intron 2 (VNTR) (STin2), 5-hydroxytryptamine (serotonin) receptor 2A gene (HTR2A) rs9526240, leptin receptor (LEPR) rs3790435) and pooled odds ratios (ORs) with 95% confidence interval (CIs); ancestry-specific effects were explored. Five studies included 3,606 participants. The overall association showed an OR = 1.25 (95%CI: 0.85-1.86; I = 76%). By ancestry, Brazilian participants of European descent demonstrated higher risk (OR = 2.80; 95%CI: 1.11-7.08), while those of West-African ancestry showed protection (OR = 0.26; 95%CI: 0.09-0.74). Genetic associations with OSA differ significantly by ancestry, supporting ancestry-informed study designs and larger multiethnic cohorts for personalized OSA management. - Source: PubMed
Publication date: 2026/09/02
Oliveira Luiz J RGuimarães Maria L RMarco Luiz DeGuimarães Nathália SBastos-Rodrigues Luciana - - Source: PubMed
Publication date: 2026/09/02
Parejo KaremJimenez-Correa UlisesDelRosso Lourdes M